ENST00000555134.2:n.996G>T
|
|
|
ENST00000556394.2:c.1612G>T
|
ENSP00000451967.2:p.Gly538Cys
|
|
ENST00000682247.1:c.2060G>T
|
ENSP00000507213.1:p.Gly687Val
|
|
ENST00000682395.1:n.2535G>T
|
|
|
ENST00000682459.1:n.1774G>T
|
|
|
ENST00000682467.1:c.1930G>T
|
ENSP00000508062.1:p.Gly644Cys
|
|
ENST00000682795.1:c.2218G>T
|
ENSP00000507574.1:p.Gly740Cys
|
|
ENST00000682895.1:n.1787G>T
|
|
|
ENST00000682955.1:n.1645G>T
|
|
|
ENST00000683188.1:c.2332G>T
|
|
|
ENST00000683380.1:n.1735G>T
|
|
|
ENST00000683907.1:c.336G>T
|
ENSP00000507754.1:n.336G>T
|
|
ENST00000684259.1:n.3838G>T
|
|
|
ENST00000684538.1:n.1450G>T
|
|
|
ENST00000684549.1:n.1622G>T
|
|
|
ENST00000261534.9:c.2071G>T
MANE Select
|
ENSP00000261534.4:p.Gly691Cys
|
|
ENST00000261534.8:c.2071G>T
|
ENSP00000261534.4:p.Gly691Cys
|
|
ENST00000452340.7:n.3047G>T
|
|
|
ENST00000554767.5:n.2857G>T
|
|
|
ENST00000555710.1:c.432G>T
|
ENSP00000451730.1:n.432G>T
|
|
ENST00000556394.1:c.126G>T
|
|
|
ENST00000556446.1:n.372G>T
|
|
|
ENST00000602717.5:c.286G>T
|
ENSP00000487704.1:p.Gly96Cys
|
|
NM_013382.5:c.2071G>T , LRG_844t1:c.2071G>T
|
NP_037514.2:p.Gly691Cys
|
|
XM_011536675.1:c.2260G>T
|
XP_011534977.1:p.Gly754Cys
|
|
XM_011536676.1:c.1927G>T
|
XP_011534978.1:p.Gly643Cys
|
|
XM_011536677.1:c.1801G>T
|
XP_011534979.1:p.Gly601Cys
|
|
XM_011536679.1:c.1354G>T
|
XP_011534981.1:p.Gly452Cys
|
|
XR_943416.1:n.2324G>T
|
|
|
XM_011536675.2:c.2260G>T
|
XP_011534977.1:p.Gly754Cys
|
|
XM_011536676.2:c.1927G>T
|
XP_011534978.1:p.Gly643Cys
|
|
XM_011536677.3:c.1801G>T
|
XP_011534979.1:p.Gly601Cys
|
|
XR_001750279.1:n.2357G>T
|
|
|
XR_001750282.1:n.3010G>T
|
|
|
XR_943416.3:n.2322G>T
|
|
|
NM_013382.6:c.2071G>T
|
NP_037514.2:p.Gly691Cys
|
|
NM_013382.7:c.2071G>T
MANE Select
|
NP_037514.2:p.Gly691Cys
|
|